510(k) K850940

ALWAYS SUPER MAXIPAD-UNSCENTED by Procter & Gamble Mfg. Co. — Product Code HHD

K850940 is an FDA 510(k) premarket notification submitted by Procter & Gamble Mfg. Co. for the device "ALWAYS SUPER MAXIPAD-UNSCENTED". The FDA issued a decision of Substantially Equivalent on May 14, 1985. The device falls under product code HHD (Pad, Menstrual, Unscented), a Class I device regulated under 21 CFR 884.5435. Procter & Gamble Mfg. Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 14, 1985
Date Received
March 7, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pad, Menstrual, Unscented
Device Class
Class I
Regulation Number
884.5435
Review Panel
OB
Submission Type

An unscented menstrual pad which is used to absorb menstrual fluid or other vaginal discharge and is made of common cellulosic and synthetic material with an established safety profile.